Transcription factor prediction database (DBD)

Transcription factor prediction database (DBD) predicts sequence-specific DNA-binding transcription factors across publicly available proteomes to support comparative and evolutionary analysis of DNA-binding domain (DBD) families.


Key Features:

  • Hidden Markov model prediction: Uses hidden Markov models to identify significant matches to sequence-specific DNA-binding domain families.
  • Proteome coverage: Provides predictions across over 700 publicly available proteomes.
  • Domain-centric annotation: Assigns DNA-binding domains to proteins and identifies DBD family membership.
  • Gene and cross-database annotations: Records gene names and includes links to external databases for predicted transcription factors.
  • Domain arrangement similarity: Reports transcription factors with similar domain arrangements.
  • Comparative distribution analysis: Characterizes the distribution of DBD families across the tree of life, including distinctions between eukaryotic and prokaryotic expansions.

Scientific Applications:

  • Evolutionary biology: Analyze DBD family distribution and expansion patterns to study transcriptional regulation evolution.
  • Functional genomics: Annotate and classify sequence-specific DNA-binding transcription factors within proteomes for functional studies.
  • Systems biology: Compare predicted transcription factor numbers relative to proteome size to infer mechanisms such as splice variant prevalence or combinatorial control strategies.

Methodology:

Hidden Markov models are applied to proteome sequences to detect significant matches to sequence-specific DNA-binding domain families.

Topics

Collections

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
10/9/2015
Last Updated:
11/24/2024

Operations

Publications

Wilson D, Charoensawan V, Kummerfeld SK, Teichmann SA. DBD––taxonomically broad transcription factor predictions: new content and functionality. Nucleic Acids Research. 2007;36(suppl_1):D88-D92. doi:10.1093/nar/gkm964. PMID:18073188. PMCID:PMC2238844.

Documentation